Showing results 5 to 8 of 8
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Title | Author(s) | Issue Date | |
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Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction Journal:Circulation: Genomic and Precision Medicine | 2020 | ||
Novel damaging mutations in CC2D1A suggest a role in human heterotaxy and ciliary dysfunction Proceeding/Conference:American Society of Human Genetics (ASHG) Virtual Meeting, 2020 | 2020 | ||
Right Ventricular Dyssynchrony in patients after Atrial Switch Operation for Transposition of the Great Arteries Proceeding/Conference:Congress of the Asian Society for Pediatric Research, ASPR 2007 | 2007 | ||
Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care Journal:European Journal of Medical Genetics | 2014 |